Canonical Allele Identifier: PA2825955427
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 961117
ClinVar RCV Id: RCV001234758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Tyr261Ser
CA375368722
NM_001162427.2:c.782A>C